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Bilateral persistent fetal vasculature due to a mutation in the Norrie disease protein gene.
Payabvash, Seyedmehdi; Anderson, Jill S; Nascene, David R.
Affiliation
  • Payabvash S; Department of Radiology, University of Minnesota, USA.
  • Anderson JS; Department of Ophthalmology, University of Minnesota, USA.
  • Nascene DR; Department of Radiology, University of Minnesota, USA nasc0001@umn.edu.
Neuroradiol J ; 28(6): 623-7, 2015 Dec.
Article in En | MEDLINE | ID: mdl-26459204
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Persistent Fetal Circulation Syndrome / Spasms, Infantile / Blindness / Genetic Diseases, X-Linked / Eye Proteins / Mutation / Nerve Tissue Proteins / Nervous System Diseases Type of study: Etiology_studies Limits: Humans / Infant / Male Language: En Journal: Neuroradiol J Year: 2015 Document type: Article Affiliation country:
Fulltext
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Print
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PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Persistent Fetal Circulation Syndrome / Spasms, Infantile / Blindness / Genetic Diseases, X-Linked / Eye Proteins / Mutation / Nerve Tissue Proteins / Nervous System Diseases Type of study: Etiology_studies Limits: Humans / Infant / Male Language: En Journal: Neuroradiol J Year: 2015 Document type: Article Affiliation country: